In vitro and in vivo studies of the novel antithrombotic agent BAY 59‐7939—an oral, direct Factor Xa inhibitor
By E. Perzborn, J. Straßburger, A. Wilmen, J. Pohlmann, S. Roehrig, Schlemmer Kh, Alexander T. Straub. Journal of Thrombosis and Haemostasis, 2005
619 citations recorded by the source corpus.
Subfields: Cardiology and Cardiovascular Medicine, Genetics, Hematology
View Paper: https://www.semanticscholar.org/paper/fff715baa620bfac1440856b95b6842a20ab2594
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In Hematology
Citations in the corpus
- The Pathogenesis of Sepsis (2011, background): “(85) describe the anti–Factor Xa activity of BAY 59–7934 (rivaroxaban), which is from a class of oxazolidinone derivatives, identified during high-throughput screening, that are competitive inhibitors of Factor Xa directed against the enzyme’s active site; they have a relatively short half-life but ”
- Safety, pharmacodynamics, and pharmacokinetics of BAY 59-7939—an oral, direct Factor Xa inhibitor—after multiple dosing in healthy male subjects (2005, background): “BAY 59-7939 is a direct FXa inhibitor and is more than 10,000-fold more selective for FXa than for other related serine proteases [ 1 ].”